rs397517368

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs397517368(A;A)

Make rs397517368(A;G)

Reference

GRCh38 38.1/141

Chromosome

21

Position

42380140

Gene

TMPRSS3

is a	snp
is	mentioned by
dbSNP	rs397517368
dbSNP (classic)	rs397517368
ClinGen	rs397517368
ebi	rs397517368
HLI	rs397517368
Exac	rs397517368
Gnomad	rs397517368
Varsome	rs397517368
LitVar	rs397517368
Map	rs397517368
PheGenI	rs397517368
Biobank	rs397517368
1000 genomes	rs397517368
hgdp	rs397517368
ensembl	rs397517368
geneview	rs397517368
scholar	rs397517368
google	rs397517368
pharmgkb	rs397517368
gwascentral	rs397517368
openSNP	rs397517368
23andMe	rs397517368
SNPshot	rs397517368
SNPdbe	rs397517368
MSV3d	rs397517368
GWAS Ctlg	rs397517368

Max Magnitude

0

ClinVar
Risk	rs397517368(A;A)
Alt	rs397517368(A;A)
Reference	Rs397517368(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	TMPRSS3
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000021.8:g.43800249C>T
CLNSRC	ClinVar
CLNACC	RCV000039330.2,